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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 357001생성일: 2026년 10월 27일

Water → 3-[4-(Imidazo[1,2-a]pyridin-5-ylthio)butyl]thiazolidine-2,4-dione

https://huagongshe.com/reaction/357001

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물ThiazolidinedioneHCID 5437—
반응물1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
반응물Imidazo[1,2-a]pyridine,5-[(4-chlorobutyl)thio]-HCID 18936641—
용매DimethylformamideHCID 6228—
생성물3-[4-(Imidazo[1,2-a]pyridin-5-ylthio)butyl]thiazolidine-2,4-dioneHCID 18936694—

반응 조건

온도80 °C

반응 단계

To a solution of 8.35 g (35.4 mmol) of 5-(4-chlorobutylthio)imidazo[1,2-a]pyridine and 4.15 g (35.4 mmol) of thiazolidine-2,4-dione in 200 ml of N,N-dimethylformamide, 5.30 ml (35.4 mmol) of 1,8-diazabicyclo[5.4.0]-7-undecene was added, followed by heating at 80° C. for 16 hours. After cooling, the reaction mixture was poured into water, extracted with ethyl acetate, washed with water and dried, after which the solvent was distilled off. The residue was purified by column chromatography (eluent: ethyl acetate). The resulting crude crystal was purified by recrystallization (solvent: chloroform/diethyl ether) to yield 10.01 g (88.0%, light orange crystal) of the desired product.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05840732
출처 데이터셋uspto-grants-1998_11
ORD IDord-52a73c16fc07454983d12e6504b1120c
출처 메모uspto-grants-1998_11